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Anatomy9

Brain Cell Line Neurofibrillary Tangles Neurofibrils Neurons COS Cells Cells, Cultured Hippocampus Cerebral Cortex

Organisms12

Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Cercopithecus aethiops Escherichia coli HIV-1 Mice, Mutant Strains Animals, Genetically Modified Saccharomyces cerevisiae Cricetinae Drosophila melanogaster Mice, Inbred BALB C

Diseases18

Disease Models, Animal Alzheimer Disease Pancreatitis, Alcoholic Parkinson Disease Genetic Predisposition to Disease Gait Ataxia Plaque, Amyloid Gaucher Disease Dementia Neurodegenerative Diseases Huntington Disease Atrophy Dementia, Vascular Nerve Degeneration Disease Progression Genetic Diseases, Inborn Syndrome Lewy Body Disease

Chemicals and Drugs36

Trypsin Inhibitor, Kazal Pancreatic Amyloid beta-Peptides Amyloid beta-Protein Precursor Serine tau Proteins Glycine Glucosylceramidase Protein-Serine-Threonine Kinases DNA Primers Presenilin-1 Recombinant Proteins Apolipoprotein E4 DNA-Binding Proteins DNA Peptide Fragments Carbamates Amyloid Precursor Protein Secretases Cysteine Codon, Nonsense Amyloid Membrane Proteins Nerve Tissue Proteins RNA, Messenger Transcription Factors Codon Apolipoproteins E Ethylnitrosourea Presenilin-2 Nuclear Proteins Neuroprotective Agents Genetic Markers Mutant Proteins Aspartic Acid Endopeptidases Bacterial Proteins alpha-Synuclein Carrier Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Animal Use Alternatives Disease Models, Animal Models, Animal Amino Acid Substitution Pedigree DNA Mutational Analysis Mutagenesis, Site-Directed Polymerase Chain Reaction Genetic Testing Models, Molecular Sequence Analysis, DNA Chromosome Mapping Models, Genetic Transfection Sequence Alignment Models, Biological Immunohistochemistry Magnetic Resonance Imaging Genetic Complementation Test Crystallography, X-Ray Case-Control Studies Cloning, Molecular Blotting, Western Reverse Transcriptase Polymerase Chain Reaction Heterozygote Detection

Psychiatry and Psychology10

Alzheimer Disease Dementia Cognition Disorders Huntington Disease Neuropsychological Tests Dementia, Vascular Mild Cognitive Impairment Lewy Body Disease Cognition Mental Status Schedule

Phenomena and Processes58

Mutation, Missense Mutation Point Mutation Amino Acid Substitution Heterozygote Frameshift Mutation Base Sequence Amino Acid Sequence Germ-Line Mutation Phenotype Genotype Alleles Genetic Predisposition to Disease Homozygote Protein Structure, Tertiary Protein Binding Mutagenesis Mutation Rate Gene Frequency Exons Binding Sites Drug Resistance, Viral Sequence Homology, Amino Acid Insecticide Resistance Protein Conformation Polymorphism, Single-Stranded Conformational Transfection Codon, Nonsense Kinetics Genetic Linkage Polymorphism, Restriction Fragment Length Protein Structure, Secondary Haplotypes Genes, Recessive Structure-Activity Relationship Sequence Deletion Genes, Dominant Gene Deletion Signal Transduction Polymorphism, Single Nucleotide Suppression, Genetic Virus Replication Aging Gene Expression Regulation Codon Genetic Variation Phosphorylation Genetic Markers Gene Expression Founder Effect Genes, p53 Epistasis, Genetic Time Factors Polymorphism, Genetic Plasmids Consanguinity Transcription, Genetic Genes, Lethal

Disciplines and Occupations1

Immunohistochemistry

Information Science4

Molecular Sequence Data Base Sequence Amino Acid Sequence Computer Simulation

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Health Care4

Genetic Testing Age of Onset Family Health Case-Control Studies

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Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care Geographicals

Animal Use Alternatives Disease Models, Animal Alzheimer Disease Models, Animal Mutation, Missense Mutation Point Mutation Amino Acid Substitution Trypsin Inhibitor, Kazal Pancreatic Pedigree Amyloid beta-Peptides Heterozygote Frameshift Mutation Molecular Sequence Data DNA Mutational Analysis Pancreatitis, Alcoholic Base Sequence Parkinson Disease Amino Acid Sequence Germ-Line Mutation Mutagenesis, Site-Directed Phenotype Genotype Alleles Amyloid beta-Protein Precursor Genetic Predisposition to Disease Homozygote Serine Jews Polymerase Chain Reaction Brain tau Proteins Genetic Testing Mice, Transgenic Cell Line Protein Structure, Tertiary Age of Onset Neurofibrillary Tangles Models, Molecular Gait Ataxia Protein Binding Mutagenesis Mutation Rate Plaque, Amyloid Gaucher Disease Sequence Analysis, DNA Gene Frequency Exons Glycine Glucosylceramidase Binding Sites Protein-Serine-Threonine Kinases DNA Primers Presenilin-1 Recombinant Proteins Mice, Inbred C57BL Drug Resistance, Viral Sequence Homology, Amino Acid Apolipoprotein E4 Insecticide Resistance DNA-Binding Proteins Protein Conformation Polymorphism, Single-Stranded Conformational Chromosome Mapping Models, Genetic Romania DNA Neurofibrils Peptide Fragments Neurons Dementia Carbamates Neurodegenerative Diseases Transfection Amyloid Precursor Protein Secretases COS Cells Cysteine Codon, Nonsense Kinetics Amyloid Sequence Alignment Genetic Linkage Polymorphism, Restriction Fragment Length Cognition Disorders Protein Structure, Secondary Models, Biological Huntington Disease Membrane Proteins Haplotypes Genes, Recessive Nerve Tissue Proteins Cells, Cultured Mice, Knockout Atrophy Cercopithecus aethiops Structure-Activity Relationship Sequence Deletion Genes, Dominant Gene Deletion Neuropsychological Tests

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